Literature review of gear-based management options in the...
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Literature review of gear-based management options in
the Caribbean for four reef fishing methods: fish traps,
spears, hook and line, and beach seines
Reef fisheries provide a vital source of income and food to millions of people worldwide. Reef fishes are
important to many countries in the Caribbean not only for their value to the fisheries, but also their
value to the tourism industry, where they are an important part of the snorkeling and diving experience.
Many Caribbean reef fisheries have been overexploited for decades and often their decline has been
accelerated by a loss of habitat. Improved management of Caribbean reef fisheries is vital to ensure
their future sustainability.
Reef fisheries in the Caribbean are difficult to manage due to the use of multiple fishing gear types, the
number of species harvested, and the dispersed landing sites used by the fishers. Additionally, there is
very little published information available on Caribbean reef fisheries and limited research into the
effects of management. This review provides a synthesis of the published literature on four gears
commonly used in Caribbean reef fisheries: fish traps, spears, hook and line, and beach seines,
summarizing evidence on best management practices for each gear. We provide brief descriptions of
each of the four gear types as well a synthesis of their use, biological impacts, and ecosystem impacts.
The management recommendations summarized below are general recommendations on gear
restrictions that could be applied to any Caribbean reef fishery.
Key recommendations for fish traps:
Minimum mesh size 3.8 cm (1.5 inch), with larger minimum mesh sizes phased in depending on
local target species – to reduce catch of juvenile fish and optimize size of target species caught.
Mandatory escape gap (or gaps) in all fish traps - to reduce catch of juveniles and bycatch
species. Two 20 x 2.5 cm gaps are one option.
Mandatory inclusion of escape panels (door held in place with biodegradable fastener) in all fish
traps - to reduce the impact of ghost fishing
Fish traps not to be set on live coral, seagrass and other sensitive habitats – to avoid damage to
corals, seagrasses and other benthic organisms
Landing-site gear disposal bins and incentive programs - to reduce disposal of damaged or
unwanted gear at sea
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Key recommendations for spearfishing:
Ban spearfishing on scuba – to avoid rapid depletion of reef fish stocks
Ban spearfishing at night – to avoid rapid depletion of reef fish stocks
Consider total ban if dive tourism is a major income source – to avoid depletion of larger fishes
and reductions in fish diversity
Key recommendation for hook and line:
If there is significant bycatch that is released, replace J-hooks with circle hooks – to reduce injury
and mortality to released bycatch
Key recommendations for beach seines:
Ban beach seine use on or near coral reefs and seagrass habitats – to avoid damage to these
sensitive habitats
Minimum mesh size 3.8 cm (1.5 inch) – to reduce proportion of juvenile fish in catch
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Contents Introduction .............................................................................................................................................. 4
Fish traps ................................................................................................................................................... 5
Description of gear and use .................................................................................................................. 5
Biological and ecosystem impacts ........................................................................................................ 6
Management options ............................................................................................................................ 6
Mesh size........................................................................................................................................... 6
Escape gaps ....................................................................................................................................... 7
Escape panels .................................................................................................................................... 8
Gear retrieval .................................................................................................................................... 9
Spearfishing ............................................................................................................................................. 10
Description of gear and use ................................................................................................................ 10
Biological and ecosystem impacts ...................................................................................................... 10
Management options .......................................................................................................................... 11
Lionfish spearfishing – new opportunities ...................................................................................... 11
Hook and line .......................................................................................................................................... 12
Description of gear and use ................................................................................................................ 12
Biological and ecosystem impacts ...................................................................................................... 12
Management options .......................................................................................................................... 13
Beach Seine ............................................................................................................................................. 13
Description of gear and use ................................................................................................................ 13
Biological and ecosystem impacts ...................................................................................................... 14
Management options .......................................................................................................................... 14
References .............................................................................................................................................. 14
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Introduction Maintaining coral reef fisheries productivity in a world where reefs are subject to multiple impacts is of
major importance to the estimated 6 million coral reef fishers worldwide who rely on these fisheries for
income and food (Teh et al., 2013). Reef fishes provide economic benefits to tourism, with tourists
willing to pay to see abundant, diverse, and large reef fish (Gill et al., 2015; Uyarra et al., 2005). Beyond
these direct economic benefits, maintaining functional reef fish communities is vital for the resilience of
coral reefs (Bozec et al., 2016; Graham et al., 2013). Coral reefs provide shoreline protection services
with an estimated value between $944 million to $2.8 billion in the Caribbean alone (Burke et al., 2011).
Retaining functional reef fish communities while balancing the demands of the coastal communities that
depend upon the reefs is an ongoing challenge for reef managers.
Reef fisheries exploit multiple species with multiple fishing gear types (Hicks and McClanahan, 2012;
McClanahan and Cinner, 2008), with catches often landed at many dispersed sites (Mahon, 1997). This
diversity of target species, gear types, and landing locations complicates fisheries monitoring and
management. Implementing marine protected areas (MPAs) is an increasingly popular way to meet both
conservation and fisheries management goals for coral reefs (Beger et al., 2015; Gaines et al., 2010).
However, gear-based management is often more readily accepted by artisanal reef fishing communities
(McClanahan et al., 2008; McClanahan and Mangi, 2004). In practice, managers use a mix of MPAs and
gear-based management for many reef fisheries (McClanahan, 2010). Gear restrictions can be tailored
to address specific fisheries issues. For example, restrictions or bans on certain gear types can protect
against habitat damage or harvesting of certain species (Cinner et al., 2009; Mangi and Roberts, 2006;
McClanahan and Mangi, 2004).
Reef fisheries in the Caribbean have been heavily depleted by past and recent overfishing (Jackson et al.,
2014; Jackson, 1997), and ensuring their future sustainability is a high priority (Salas et al., 2007).
Although many countries within the Caribbean already have some regulations on the use of fishing gear
(McManus and Lacambra, 2005), there is little published advice on what gear-based management
options are available. This review aims to provide an outline of four common fishing gear types used on
and near Caribbean reefs (fish traps, spears, hook and line, and beach seines) and includes a summary of
current understanding of the biological and ecosystem impacts of these gears and the management
options available. We focus specifically on gear restrictions, such as minimum mesh sizes for traps and
nets, and bans on the use of gears in certain habitats. There are many other management options
available that can be used in combination with these measures, such as minimum landing sizes,
individual quotas, and marine reserves.
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Fish traps Description of gear and use
Fish traps were the predominant gear in Caribbean reef fisheries
15 years ago (Fig. 1; Mahon and Hunte, 2001; Munro, 1983), and
this is still the case on many islands today (CRFM, 2014). Traps
are popular with reef fishers within the Caribbean as they are
relatively simple and inexpensive to make (Garrison and Beets,
1998). They can be used on rugged substrates where other gears
might be damaged (Miller and Hunte, 1987). Also, they catch fish
without the fisher having to attend them and, as such, can be left
at sea in inclement weather (Hawkins et al., 2007). The most
frequently used traps are the Antillean Z-trap and the arrowhead
or chevron trap (Mahon and Hunte, 2001) (Fig. 2). S-traps and
rectangular traps are also in use, mainly in Cuba and Puerto Rico,
respectively (Mahon and Hunte, 2001).
Figure 2. Two most common types of Caribbean fish traps: (a) single funnel arrowhead or chevron trap; (b) the double funnel Antillean Z-trap (from Munro et al., 1971)
Traps are usually set on or near reefs but may also be deployed in deeper water to catch snappers and
groupers found at depth (Mahon and Hunte, 2001). Physical characteristics of the trap, fishing methods,
fish biology and ecology, and environmental factors each affect trap catch rates (Table 1). Traps catch a
high diversity of reef fish, with as many as 90 species and 35 families recorded in the Caribbean over
multiple trap hauls (Jiménez and Sadovy, 1996), including species from most reef fish families. Snappers
(Lutjanidae) and groupers (Serranidae) are typically the target species for Caribbean reef fisheries, but
Figure 1. Multi-species trap catch in Barbados. Photo credit: Hazel Oxenford
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the Caribbean-wide depletion of these fish families has resulted in ‘fishing down the food web’, with
increasing proportions of lower trophic level species such as parrotfish (Scaridae) and surgeonfish
(Acanthuridae) being targeted (Garrison and Beets, 1998; Johnson, 2010).
Table 1. Trap characteristics that can affect catch rates and species composition of catch (principally from Mahon & Hunte 2001)
Physical characteristics Fishing method Fish biology and ecology Environmental factors
Mesh size
Trap design
Trap size
Escape gaps
Soak time*
Depth
Bait
Location of traps
Fish behavior
Predation
Mobility and activity of fishes
Body size and shape of fishes
Moon phase
Shelter provided by trap
Visibility
*Length of time traps are left underwater before fish are harvested
Biological and ecosystem impacts
For fisheries managers, traps present a considerable challenge as they can impact fish stocks and
ecosystems in a number of different ways. First, the small mesh sizes that are frequently used in traps
result in the capture of juvenile fishes. Second, traps have poor selectivity – they will retain any fish that
enters the trap and is not able to find its way back out of the entrance funnel or escape through the
mesh. This indiscriminate harvest results in high catch diversity and the capture of many species that are
not of commercial interest. Third, fish traps catch herbivorous fish, including parrotfish (Scaridae) and
surgeonfish (Acanthuridae), which play a vital role in facilitating coral growth and recovery by controlling
the abundance of macroalgae on reefs (Mumby, 2006; Mumby and Harborne, 2010). Fourth, traps
themselves can cause direct physical damage to habitats, such as scarring or breaking corals (Marshak et
al., 2007). Finally, traps are frequently lost or abandoned. These traps will continue to catch fish for as
long as their physical structure is intact (called “ghost fishing”), contributing to fish mortality rates.
Management options
Mesh size
The mesh size of a trap plays an important role in determining the size of fish caught and the species
composition of catch, likely due to size selectivity (Mahon and Hunte, 2001). Regulation of mesh size is
therefore used as a method of reducing the proportion of juvenile fish in trap catches and for increasing
the number of large fish that have greater commercial value (Baldwin et al., 2004; Bohnsack et al.,
1989). Given the high diversity of species caught in fish traps, no single mesh size can avoid catching all
juvenile fish while also maximizing the yield of every species. The best mesh size to ensure sustainable
catches of one target species may still lead to overfishing of other species. The experimental data
available on mesh sizes is limited, but the body of evidence suggests that an increase in mesh size to 3.8
cm can result in an increase in catch weight per unit effort in the long term (though this may take a year
or more) and a reduction in immature fish in the catch (Mahon and Hunte, 2001; Sary et al., 1997).
Increasing mesh size to 5.1 cm can further reduce the proportion of immature fish and may be optimal
for some species, e.g. silk snapper (Lutjanus vivanus) (Wolf and Chislett, 1974). There are no long-term
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experiments with 5.1 cm mesh size traps, so it is not known what effects adopting such a mesh size
would have on long-term fisheries sustainability. If larger mesh sizes are introduced, a phased
introduction of progressively larger sizes can help avoid excessive hardship for fishers due to large
reductions in catch in the short term (Mahon and Hunte, 2001).
Most research to determine the effect of mesh size on catches has been conducted where trap fishing
already takes place and where the mesh sizes used in the existing fishery are smaller than those being
used in the research study (Mahon and Hunte, 2001). Most of these studies find that larger mesh sizes
lead to a reduction in catch per trap. However, this result is to be expected given the smaller mesh size
traps that fishers use will catch most fish before they reach a size when they could be caught in the
larger mesh traps used in experiments. To understand the effect an increase in mesh size would have on
catches, it is necessary to modify or replace all (or nearly all) traps in a fishery with the desired mesh size
and follow the change in catch over several years.
The only experiments to look at longer-term effects of increased mesh sizes in the Caribbean showed
that the mean catch weight per trap per haul for a 1.5 inch (3.8 cm) mesh one year after introduction
was almost the same (0.83 kg) as that for the 1.25 inch (3.2 cm) mesh in the previous year (0.79 kg; Sary
et al., 1997). Catch for the larger mesh traps increased to 1.24 kg three years after introduction. The
mean length of Redband Parrotfish (Sparisoma aurofrenatum) was higher in the large mesh traps,
indicating that the catch of juveniles and smaller individuals of this species was reduced (Sary et al.,
1997).
Escape gaps
Figure 3. View of trap underwater with escape gap visible on the right hand-side of the image. Photo: https://www.rare.org/stories/2011-solution-search-winners
Compared to mesh size, relatively little research has been published on the effects of escape gaps on
trap catches (Johnson, 2010; Munro et al., 2003). Escape gaps are narrow slits that are built into a trap
(Fig. 3), with tested sizes varying from short gaps, e.g. 7 x 2.5 cm, to taller gaps, e.g. 40 x 2.5 cm, and
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widths varying from 2 cm to 8 cm (Baldwin et al., 2004; Condy et al., 2015; Johnson, 2010). The use of
escape gaps offers a complementary or alternative approach to increased mesh size by adjusting the
size selectivity of traps and allowing juveniles and narrow-bodied fish to escape. The few research
studies that have evaluated the use of escape gaps have found the value of catches may be maintained
or reduced in the short-term and increased in the longer-term.
The most recent Caribbean study, in Curaçao, tested short escape gaps (20 x 2.5 cm) and tall escape
gaps (40 x 2.5cm). Both sizes resulted in decreased catches of key herbivores (-58% and -50%,
respectively) and bycatch species, such as butterflyfish and damselfish (-74% and -80%), and increases in
the mean length of fish caught (Johnson, 2010). Furthermore, no significant reduction in the catch of
high-value fish or market value of the catch was found with these escape gaps, though mean weight of
the total catch was reduced.
These results are generally consistent with two studies based in Kenya that examined the performance
of traps with escape gaps of varying sizes (Condy et al., 2015; Gomes et al., 2014). Both Kenya studies
found reductions in the abundance of juvenile fish in the catch and an increased proportion of more
commercially valuable adult species. One of these studies predicted a decline in profitability in the first
year if escape gaps were implemented, with an increase in following years (Condy et al., 2015). The
second study found no change in value of the catch in heavily fished areas and an increase in value in
less depleted areas (Gomes et al., 2014).
Escape panels
In some fisheries 20-30% of traps are lost, abandoned, or discarded per year (NOAA Marine Debris
Program, 2015), resulting in millions of ghost fishing traps worldwide (Scheld et al., 2016). Escape
panels, which are weighted panels with a biodegradable fastener, have emerged as the best option for
reducing the impacts of ghost fishing by traps (Stewart, 2007; Selliah et al., 2001; Fig. 4). Hemp twine
has been shown to be the most suitable material for the fastener within the Caribbean (Selliah et al.,
2001). Escape panels tied with hemp twine and weighted to help the panel fall open, opened after 22 -
26 days during testing (Selliah et al., 2001).
Figure 4. Arrowhead trap showing escape panel (after Renchen et al. 2014)
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The only Caribbean study on the effects of trap ghost fishing took place in the U.S. Virgin Islands
(U.S.V.I.) and documented a 2% mortality rate for trapped fish (Renchen et al., 2014). Another study in
Florida, not specifically focused on ghost fishing, found that 27% of fish were dead or injured in traps left
for 20 days, and 17% of fish in traps left for two months were dead or injured (Taylor and McMichael,
Jr., 1983). Neither experiment includes estimates of fish mortality through predation and scavenging
within the cage, which may be a significant (Munro et al., 1971; Rassweiler and Rassweiler, 2011).
Estimates of trap losses are variable with 10% of traps estimated to be lost each year in the U.S.V.I.
(Renchen et al., 2014) and 15-20% lost per 20-day trip in the Tortugas, Florida (Taylor and McMichael,
Jr., 1983). The use of escape panels was found to reduce fish mortality to near zero (Renchen et al.,
2014). Escape panels are required by law in all traps used in Barbados (Baldwin et al., 2004), Curaçao,
Puerto Rico and the U.S. Virgin Islands (NOAA, CFMC, 2015).
Gear retrieval
One option to further reduce ghost fishing pressure in an area, is to remove traps that have been
abandoned or lost at sea. In Chesapeake Bay, the removal of 34,408 derelict crab pots (9% of derelict
gear in Virginia waters) led to an estimated additional 13, 504 MT of harvest (27% more than if no
removals had occurred) with a value of US $21.3 million (Scheld et al., 2016). In addition to contributing
to fish mortality, derelict gear can cause mortality and injuries of marine mammals and turtles (Stokes et
al., 2011).
Finding and removing derelict fishing gear (nets, traps, and other gear that has been discarded,
abandoned, or lost) is challenging, but several studies have used side-scan sonar, Scuba diver surveys,
and towed cameras to locate traps (Arthur et al., 2014). The success of these methods is dependent on
several factors. Scuba surveys and cameras are generally only effective in shallow, clear waters (though
cameras on remotely operated vehicles can be used in deeper waters), and sonar is less effective in
areas with rugose-bottom environments (Arthur et al., 2014). Once located, divers can retrieve derelict
gear, though care is required that they do not become entangled and that damage to sensitive
substrates is minimized. Another option is to use a grappling hook suspended from a boat to attempt to
snag gear and then pull it to the surface. In cases where the trap has become substantially encrusted
with corals or other benthic organisms, but is no longer ghost fishing, there may be cause to leave traps
in place.
To encourage fishers not to dispose of their gear at sea, there should be affordable facilities at ports for
proper disposal of fishing gear, or even incentive programs (NOAA Marine Debris Program, 2015). For
example, the Republic of Korea offers about US$10 per 100 liter bag of fishing gear as an incentive for
the proper disposal of gear, and collected 5,137 tonnes of gear in 2006 (Macfadyen et al., 2009). Similar
schemes could help reduce disposal of gear at sea within the Caribbean.
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Spearfishing
Description of gear and use
Spearfishing normally involves the use of a rubber-propelled
spear operated by a person swimming at or below the
surface (Ennis and Aiken, 2014; Frisch et al., 2007).
Spearfishers commonly free dive (dive without tanks; Fig. 5)
but may also use scuba or hookah equipment (surface-
supplied air systems). Despite being banned or regulated on
many islands, few published studies or descriptions exist on
spearfishing in the Caribbean (Gillett and Moy, 2006). One of
the few studies to quantify spearfishing in the region
estimates that the proportion of spearfishers in Jamaica has
grown from 1% of all types of fishers in 1991 to 10% in 2011
(Ennis and Aiken, 2014). Landings from spearfishers are likely
an under-recorded portion of reef fishery landings, as
demonstrated in Barbados where one study estimated that
annual landings from spearfishing exceeded the official
landings total for the entire reef fishery (Simpson et al.,
2013).
Biological and ecosystem impacts
Spearfishing can be an efficient method of harvesting fish. It is highly selective as spearfishers are able to
target species and sizes of fish directly, which results in much lower bycatch compared to other fishing
methods (Dalzell, 1996; Frisch et al., 2012). While this is good news for non-target species, this
selectivity can lead to reductions in the mean size and abundance of target species (Chapman and
Kramer, 1999; Frisch et al., 2012). Such changes are exemplified by a study on the Great Barrier Reef
that found a 54% reduction in density and a 27% reduction in mean size of coral trout (Plectropomus
spp.) three years after spearfishing was first permitted (Frisch et al., 2012). Although the targeting of
larger individuals generally avoids the problem of removing fish before they are able to reach maturity,
the largest (oldest) fish often have greater reproductive potential in the form of greater numbers of eggs
produced and higher survival rates in their larvae, compared to younger fish. (Birkeland and Dayton,
2005).
Large fish have other ecosystem benefits as well. For example, large parrotfish have a
disproportionately greater algal grazing intensity than small parrotfish. As noted previously, herbivores
such as parrotfish are vital to the maintenance of reefs in a coral-dominated state (Mumby et al., 2006).
As such, the impacts of reduced grazing intensity might be particularly severe in areas where parrotfish
are targeted directly, such as Barbados (Simpson et al., 2013).
Figure 5. Spearfisher with catch of reef fish at Glitter Bay, Barbados. Photo credit: David Gill
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Management options
Current management of spearfishing in the Caribbean has focused on totals bans on spearfishing gear
and bans on spearfishing while on scuba or hookah, as well as regulations requiring spearfishers to
obtain permits (Gillett and Moy, 2006; McManus and Lacambra, 2005). Bans on spearfishing at night
have also been implemented as some species of reef fish sleep on the reef at night and therefore make
easy targets. Jamaica and many places in the Pacific prohibit spearfishing at night, though these bans
are difficult to enforce (Ennis and Aiken, 2014; Gillett and Moy, 2006). In areas where tourism is a
significant source of income, there may be support for total bans on spearfishing, e.g. the Dutch
Caribbean and U.S. Virgin Islands already ban spearfishing (Gillett and Moy, 2006). These bans can help
protect reef biodiversity which tourists, especially dive tourists, want to see (Gill et al., 2015; Uyarra et
al., 2005). Many Caribbean countries that do not have bans are considering one (Gillett and Moy, 2006).
Lionfish spearfishing – new opportunities
In Bonaire, where spearfishing has been banned, the national parks authority has issued permits to
recreational divers that allow them to use a modified spear gun to kill lionfish (de León et al., 2013).
Lionfish are an invasive species within the Caribbean and can have significant ecosystem impacts. The
lionfish preys on a wide diversity of reef fishes and can rapidly decrease the biomass of their prey (Albins
and Hixon, 2011; Green et al., 2012), and, with no local predators, their population growth has been
explosive (Green and Côté, 2008).
To reduce lionfish populations, sustained removals are required (Barbour et al., 2011) and therefore
there may be the potential to develop lionfish fisheries. Any attempts to develop such a fishery should
proceed carefully, as spearfishing of lionfish can still have negative impacts such as physical damage to
reefs from divers and their spears, and, in areas where spearfishing has been banned, spearfishers may
poach other species. There is also concern that lionfish can contain the ciguatera toxin, a lipid soluble
toxin produced by microalgae, that can cause poisoning in humans (Dickey and Plakas, 2010). However,
no cases of poisoning due to lionfish consumption have been reported within the Caribbean (Wilcox and
Hixon, 2014). Despite these potential issues, if properly regulated, a targeted lionfish fishery could
potentially benefit the reef ecosystem in addition to providing a new fish species for market.
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Hook and line
Figure 6. Fishing line with rock as weight being prepared for fishing in Tobago. Note multiple baited hooks. Photo credit: Jason Flower
Description of gear and use
Hook and line fishing (‘line fishing’) refers to the use of a fishing line (made from natural or synthetic
material) with a hook or hooks attached which may be baited. ‘Bottom fishing’, a type of line fishing
common in and around reefs, entails a weighted line and one or more baited hooks lowered to the
seafloor (Fig. 6; Munro, 1983). Target species are generally demersal reef species and deep slope
species, such as groupers and snappers (Mumby et al., 2014), and fishing depths can range from shallow
reefs (< 45 m) to deep banks that may be in 30-250 m of water (Munro, 1983). Line fishing for pelagic
species such as tunas and Wahoo is also practiced using a variety of methods; however, these are not
covered here as they are not generally associated with reefs. In the 1980s, line fishing was the second
most important method of reef fish exploitation in the Caribbean (Munro, 1983), and national reports
from some countries, such as Grenada and Jamaica, suggest this may still be the case today (CRFM,
2014).
Biological and ecosystem impacts
Line fishing is the least regulated of all fishing methods in the Caribbean and little information is
available on its impacts on coral reefs. Compared to trap fishing and beach seining, line fishing’s direct
physical impact on habitat is minimal, although the weight used to keep the line vertical and the line
itself may cause damage to corals and other benthic organisms (Chiappone et al., 2002). Additionally,
fishing lines can entangle marine mammals and turtles, and hooks can be ingested causing injuries and
mortality (Stokes et al., 2011). Line fishing catches from reefs generally avoid ecologically important
herbivores and are composed mainly of snappers, groupers, and grunts (Dalzell, 1996).
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Management options
Circle hooks can reduce the injury to and mortality of juvenile and other non-target fish that are
inadvertently captured and then released. Circle hooks are similar to the more commonly used J hooks
(Fig. 7), but the point is turned back towards the shank forming a generally circular shape (Cooke and
Suski, 2004). They have been shown to reduce the mortality rates for several species when compared to
J hooks by more frequently hooking fish in the jaw rather than in the gut (Cooke and Suski, 2004; Sauls
and Ayala, 2012). The use of circle hooks was mandated in the U.S. federal waters of the Gulf of Mexico
in 2007 in an effort to reduce bycatch mortality (Garner et al., 2014). Hook size can also affect the size of
species caught and catch composition, and there is some evidence larger hook sizes increase the mean
length of the catch. However, larger hooks may also reduce catch rates (Garner et al., 2014; Sauls and
Ayala, 2012).
Figure 7. Two circle hook designs (a,b) and a conventional J-style hook (c) (after Cooke and Suski, 2004)
Beach Seine Description of gear and use
Beach seine nets consist of a rectangular
wall of netting (Fig. 8) that is held
vertical in the water by floats at the
surface and weights at the bottom
(Adams, 1993). One end of the net is
held at the beach while the rest of the
net is played out by a boat, setting the
net in a semi-circle around the targeted
fish. The boat brings the other end of the
net in further down the shoreline and
the net is pulled in towards the shore in
an ever decreasing semi-circle that
encloses the fish. Nets can be tens to
hundreds of meters long (Adams, 1993; Figure 8. Sorting a beach seine catch in Charlotteville, Tobago. Photo credit: Jason Flower
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Maraj et al., 2011). The main species caught by beach seines include small coastal pelagic species such
as scads (Decapterus spp. and Selar crumenopthalmus) and small jacks (Caranx spp.) as well as small
demersal species and immature reef fishes. Beach seine nets are commonly used throughout the Lesser
Antilles (CRFM, 2014; Mahon, 1993; Munro, 1983).
Biological and ecosystem impacts
Two impacts are of particular concern with the use of beach seines: the non-selective nature of the nets
and habitat damage caused by dragging gear. Seine nets catch a high diversity of fish and many juveniles
(Mangi and Roberts, 2006; McClanahan and Mangi, 2004). In Kenya, more than two-thirds of beach
seine catches were composed of juvenile fish (Mangi and Roberts, 2006). In the same study, researchers
found that beach seine use impacted coral cover and diversity, as the nets and team of fishers (including
snorkelers) came into contact with corals. Although fishers using beach seine will not actively target
rocky substrate, such as reefs, nearshore areas in the Caribbean often have cover of seagrass and corals,
and setting and dragging a seine net through these can result in significant damage and loss of habitat.
Management options
In areas in Kenya where beach seines have been banned, other fishing gears have shown increases in
catches (McClanahan, 2010). A total ban may not be an option in places where beach seine fishing is an
important source of income and protein (Fanning and Oxenford, 2011). In these instances, policymakers
could prohibit seining in coral and seagrass beds to avoid damage to those habitats, e.g. Barbados bans
the use of beach seines near coral reefs (McManus and Lacambra, 2005). As with traps, a minimum
mesh size for seine nets could help reduce the proportion of juvenile fish in catches. Several countries in
the Caribbean have regulated the mesh size of beach seine nets. In St. Lucia, the minimum mesh size is
31.75 mm (1.25 inches), while Antigua and Barbuda as well as Barbados have a 38.1 mm (1.5 inches)
minimum mesh size (McManus and Lacambra, 2005).
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